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Entropy-driven durability enhancement of PtM<sub>3</sub> (M = transition metal) type alloy catalysts for the oxygen reduction reaction

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dc.contributor.authorWang, Jiaqi
dc.contributor.authorZhang, Longhai
dc.contributor.authorLiang, Jinhui
dc.contributor.authorTu, Yuanhua
dc.contributor.authorSong, Huiyu
dc.contributor.authorXiang, Yan
dc.contributor.authorYang, Nianjun
dc.contributor.authorLiao, Shijun
dc.contributor.authorCui, Zhiming
dc.contributor.orcidext0000-0001-6147-657X
dc.date.accessioned2026-07-09T13:21:23Z
dc.date.available2026-07-09T13:21:23Z
dc.date.createdwos2026-03-01
dc.date.issued2026
dc.description.abstractLow-platinum (low-Pt) alloys are widely regarded as a promising alternative to commercial Pt/C catalysts, owing to their excellent balance of cost reduction and enhanced catalytic performance. However, they have long been hindered by a critical challenge—poor durability—primarily stemming from the dissolution of non-noble metals. Herein, we report a series of high-performance, stable low-Pt high-entropy intermetallic catalysts with the composition Pt(FeCoNi)3−xInx (where x = 0.25, 0.5, 0.75, 1), and systematically elucidate the role of entropy in regulating both the dissolution behavior of non-noble metals and the overall catalytic performance. The optimized high-entropy intermetallic Pt(FeCoNi)2.5In0.5 (PFCNI) exhibited significantly superior stability to its binary counterparts. PFCNI delivered an initial mass activity of 1.04 A mgPt−1, with only a 14.3% loss after 30 000 accelerated durability test (ADT) cycles—outperforming both commercial Pt/C and the binary reference catalysts. When integrated into a membrane electrode assembly (MEA), PFCNI retained 74.1% of its maximum power density after 30 000 accelerated stress test (AST) cycles. In contrast, the MEA based on PtNi3 (a binary counterpart) retained merely 16.8% of its maximum power density even after a shorter duration of 20 000 AST cycles. This study demonstrates that the high-entropy effect remarkably enhances the stability of typical PtM3-type catalysts for the acidic oxygen reduction reaction (ORR), thereby offering a promising strategy for the development of low-Pt catalysts with long-term durability.
dc.description.wosFundingTextThis work was financially supported by the National Natural Science Foundation of China (22372062, 22572062 and U22A20419) and the Key Technologies R&D Program of Guangdong Province (2023B0909060003).
dc.identifier.doi10.1039/d5ta09697a
dc.identifier.eissn2050-7496
dc.identifier.issn2050-7488
dc.identifier.issn2050-7496
dc.identifier.urihttps://imec-publications.be/handle/20.500.12860/59802
dc.language.isoeng
dc.provenance.editstepusergreet.vanhoof@imec.be
dc.publisherROYAL SOC CHEMISTRY
dc.source.beginpage12014
dc.source.endpage12024
dc.source.issue20
dc.source.journalJOURNAL OF MATERIALS CHEMISTRY A
dc.source.numberofpages11
dc.source.volume14
dc.subject.keywordsFUEL-CELL STACK
dc.subject.keywordsNANOPARTICLES
dc.title

Entropy-driven durability enhancement of PtM3 (M = transition metal) type alloy catalysts for the oxygen reduction reaction

dc.typeJournal article
dspace.entity.typePublication
imec.internal.crawledAt2026-02-20
imec.internal.sourcecrawler
imec.internal.wosCreatedAt2026-04-07
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